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On-line Access: 2024-08-27
Received: 2023-10-17
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Sunjian LYU, Xuemei YUAN, Li LIU, Haiqi ZHANG, Zhe YU, Xiaoying HANG, Weida SHI, Yinglei WU. Application of a recombinant replicase to localize the Trionyx sinensis hemorrhagic syndrome virus and evaluate its effects on antiviral genes of T. sinensis[J]. Journal of Zhejiang University Science B, 2021, 22(4): 295-304.
@article{title="Application of a recombinant replicase to localize the Trionyx sinensis hemorrhagic syndrome virus and evaluate its effects on antiviral genes of T. sinensis",
author="Sunjian LYU, Xuemei YUAN, Li LIU, Haiqi ZHANG, Zhe YU, Xiaoying HANG, Weida SHI, Yinglei WU",
journal="Journal of Zhejiang University Science B",
volume="22",
number="4",
pages="295-304",
year="2021",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B2000504"
}
%0 Journal Article
%T Application of a recombinant replicase to localize the Trionyx sinensis hemorrhagic syndrome virus and evaluate its effects on antiviral genes of T. sinensis
%A Sunjian LYU
%A Xuemei YUAN
%A Li LIU
%A Haiqi ZHANG
%A Zhe YU
%A Xiaoying HANG
%A Weida SHI
%A Yinglei WU
%J Journal of Zhejiang University SCIENCE B
%V 22
%N 4
%P 295-304
%@ 1673-1581
%D 2021
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B2000504
TY - JOUR
T1 - Application of a recombinant replicase to localize the Trionyx sinensis hemorrhagic syndrome virus and evaluate its effects on antiviral genes of T. sinensis
A1 - Sunjian LYU
A1 - Xuemei YUAN
A1 - Li LIU
A1 - Haiqi ZHANG
A1 - Zhe YU
A1 - Xiaoying HANG
A1 - Weida SHI
A1 - Yinglei WU
J0 - Journal of Zhejiang University Science B
VL - 22
IS - 4
SP - 295
EP - 304
%@ 1673-1581
Y1 - 2021
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B2000504
Abstract: Trionyx sinensis Hemorrhagic Syndrome Virus (TSHSV) is an arterivirus newly discovered in Chinese softshell turtles. Little is known about the effect of antibodies against the virus or the distribution of the virus in different organs of infected turtles. In this study, a partial protein of TSHSV-HP4 was produced using a prokaryotic expression system, and its polyclonal antibody was generated. The polyclonal antibody was confirmed by western blot and dot enzyme-linked immunosorbent assay (dot-ELISA). The distribution of TSHSV in different organs of T. sinensis was examined by immunohistochemistry (IHC) and the expression of immune-related genes was analyzed using quantitative real-time polymerase chain reaction (qRT-PCR). The results indicated that the recombinant TSHSV-HP4 protein was successfully expressed, and the generated polyclonal antibody showed specific binding to viral particles in the lung tissues of infected turtles. The IHC assay indicated that the virus was highly localized in various cells, including intestinal lymphocytes, enterocytes, kidney epithelial cells, spleen cells, lung macrophages, and cardiomyocytes. The qRT-PCR analysis revealed that TSHSV was detected in all organs tested, including the lungs, liver, kidneys, spleen, and heart. The numbers of viral mRNA copies in lung and heart tissues were significantly higher in the virus-antibody group than in the virus group. The interferon-stimulated genes (ISGs), myxovirus resistance protein 2 (MX2) and radical S-adenosyl methionine domain containing 2 (RSAD2) were highly upregulated in all groups of infected turtles. Antibody-dependent enhancement (ADE) seemed to occur after stimulation by the polyclonal antibody, because significantly greater expression of the two genes was detected in the virus-antibody group than in the virus group. Overall, these results are important in understanding the cell localization of TSHSV and the immune response of infected turtles.
[1]ChenZ, ZhangMH, ZhouXP, et al., 2017. Development and detection application of monoclonal antibodies against Zucchini yellow mosaic virus. J Integr Agric, 16(1):115-124.
[2]DejnirattisaiW, JumnainsongA, OnsirisakulN, et al., 2010. Cross-reacting antibodies enhance dengue virus infection in humans. Science, 328(5979):745-748.
[3]FangJY, WangHY, BaiJ, et al., 2016. Monkey viperin restricts porcine reproductive and respiratory syndrome virus replication. PLoS ONE, 11(5):e0156513.
[4]FangY, SnijderEJ, 2010. The PRRSV replicase: exploring the multifunctionality of an intriguing set of nonstructural proteins. Virus Res, 154(1-2):61-76.
[5]Fishery Administration Bureau of Ministry of Agriculture and Rural Areas, National Aquatic Technology Extension Station, China Society of Fisheries, 2018. China Fishery Statistical Yearbook. China Agriculture Press, Beijing, China, p.24 (in Chinese).
[6]GirnJ, KavoosiM, ChantlerJ, 2002. Enhancement of coxsackievirus B3 infection by antibody to a different coxsackievirus strain. J Gen Virol, 83(2):351-358.
[7]KnoopsK, KikkertM, van der WormSHE, et al., 2008. SARS-coronavirus replication is supported by a reticulovesicular network of modified endoplasmic reticulum. PLoS Biol, 6(9):e226.
[8]KurokawaC, IankovID, GalanisE, 2019. A key anti-viral protein, RSAD2/VIPERIN, restricts the release of measles virus from infected cells. Virus Res, 263:145-150.
[9]KvisgaardLK, LarsenLE, HjulsagerCK, et al., 2017. Genetic and biological characterization of a Porcine Reproductive and Respiratory Syndrome Virus 2 (PRRSV-2) causing significant clinical disease in the field. Vet Microbiol, 211:74-83.
[10]LiuL, CaoZ, LinF, et al., 2015. Partial sequence of a novel virus isolated from Pelodiscus sinensis hemorrhagic disease. Intervirology, 58(4):197-204.
[11]LiuL, CaoZ, LinF, et al., 2017. The histopathological characteristics caused by Trionyx sinensis hemorrhagic syndrome virus (TSHSV) and comparative proteomic analysis of liver tissue in TSHSV-infected Chinese soft-shelled turtles (Pelodiscus sinensis). Intervirology, 60(1-2):19-27.
[12]LiuL, WeiQ, LinQQ, et al., 2019. Anti-spike IgG causes severe acute lung injury by skewing macrophage responses during acute SARS-CoV infection. JCI Insight, 4(4):e123158.
[13]LyuSJ, YuanXM, ZhangHQ, et al., 2019. Complete genome sequence and analysis of a new lethal arterivirus, Trionyx sinensis hemorrhagic syndrome virus (TSHSV), amplified from an infected Chinese softshell turtle. Arch Virol, 164(10):2593-2597.
[14]LyuSJ, YuanXM, ZhangHQ, et al., 2020. Transcriptome profiling analysis of lung tissue of Chinese soft-shell turtle infected by Trionyx sinensis Hemorrhagic Syndrome Virus. Fish Shellfish Immunol, 98:653-660.
[15]McGillivaryG, JordanZB, PeeplesME, et al., 2013. Replication of respiratory syncytial virus is inhibited by the host defense molecule viperin. J Innate Immun, 5(1):60-71.
[16]MeierK, Jaguva VasudevanAA, ZhangZL, et al., 2018. Equine MX2 is a restriction factor of equine infectious anemia virus (EIAV). Virology, 523:52-63.
[17]ParkH, JungS, ShinH, et al., 2019. Localization and persistence of hepatitis A virus in artificially contaminated oysters. Int J Food Microbiol, 299:58-63.
[18]QadiriSSN, KimSJ, KrishnanR, et al., 2019. Localization and tissue tropism of viral haemorrhagic septicemia virus (VHSV) in experimentally infected juvenile olive flounder, Paralichthys olivaceus: an in situ hybridization and immunohistochemical study. Aquaculture, 505:242-252.
[19]SiLL, GuoXL, GuoPJ, et al., 2016. Neutralizing effect and antibody dependent enhancement activity of anti-DENV prM polyclonal antibody. J Sun Yat-Sen Univ (Med Sci), 37(3):321-325 (in Chinese).
[20]TiradoSMC, YoonKJ, 2003. Antibody-dependent enhancement of virus infection and disease. Viral Immunol, 16(1):69-86.
[21]VairoS, SaeyV, BombardiC, et al., 2014. The recent European isolate (08P178) of equine arteritis virus causes inflammation but not arteritis in experimentally infected ponies. J Comp Pathol, 151(2-3):238-243.
[22]WanYS, ShangJ, SunSH, et al., 2020. Molecular mechanism for antibody-dependent enhancement of coronavirus entry. J Virol, 94(5):e02015-19.
[23]WangHY, BaiJ, FanBC, et al., 2016. The interferon-induced Mx2 inhibits porcine reproductive and respiratory syndrome virus replication. J Interferon Cytokine Res, 36(2):129-139.
[24]WangXY, HinsonER, CresswellP, 2007. The interferon-inducible protein viperin inhibits influenza virus release by perturbing lipid rafts. Cell Host Microbe, 2(2):96-105.
[25]WenJQ, ChengYF, LingRS, et al., 2020. Antibody-dependent enhancement of coronavirus. Int J Infect Dis, 100:483-489.
[26]YipMS, LeungNHL, CheungCY, et al., 2014. Antibody-dependent infection of human macrophages by severe acute respiratory syndrome coronavirus. Virol J, 11:82.
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